Fingerprint
Dive into the research topics of 'Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia
Evgeny A Glazov, Andreas Zankl, Marina Donskoi, Tony J Kenna, Gethin P Thomas, Graeme R Clark, Emma L Duncan, Matthew A Brown
Research output: Contribution to journal › Article › peer-review
63
Citations
(Scopus)
7
Downloads
(Pure)